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An Adaptive Clinical Trial of BeginNGS Newborn Screening for Hundreds of Genetic Diseases by Genome Sequencing

NCT06306521

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

The goal of this clinical trial is to test a new method for newborn screening using whole genome sequencing, called BeginNGS. Parents will be approached to provide informed consent to enroll their newborns in prenatal, postnatal, and outpatient settings. The main questions this study aims to answer are: What is the utility of BeginNGS as compared to state newborn screening? What is the acceptability and feasibility of BeginNGS as compared to state newborn screening? What is the cost effectiveness of BeginNGS as compared to state newborn screening?

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Genetic Disease

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
1 day to 28 days
Sex
All
Healthy volunteers
Accepted
Sponsor
Rady Pediatric Genomics & Systems Medicine Institute
Last updated on ClinicalTrials.gov
March 12, 2024

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • Rady Children's Hospital San Diego · San Diego, CA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.